Di/qc & Admin Lead

Johnson & Johnson

Santa Clara, California, United States of America
Base: $150,000 - $170,000; bonus/equity: eligible ...
Hybrid
21 cfr part 58 compliance expertise
Good laboratory practices glp oversight
Data integrity review of study files
This role supports the execution of preclinical studies required to competitively position robotic and digital solutions for regulatory approval

Job Summary

  • This role supports the execution of preclinical studies required to competitively position robotic and digital solutions for regulatory approval.
  • The incumbent will serve as a Subject Matter Expert on 21 CFR Part 58 to provide compliance oversight for preclinical research staff.
  • Employees are eligible for comprehensive benefits including medical, dental, vision, 401(k), and up to 480 hours of parental leave.

Matching Summary

This role supports the execution of preclinical studies required to competitively position robotic and digital solutions for regulatory approval.

Salary

Base: $150,000 - $170,000; Bonus/Equity: Eligible for long-term incentive program; Benefits: Medical, dental, vision, 401(k), vacation, sick time, and parental leave

Skills & Requirements

Must-have

  • 21 CFR Part 58 compliance expertise
  • Good Laboratory Practices GLP oversight
  • Data integrity review of study files
  • Animal facility quality control processes
  • Deviation tracking and corrective actions

Nice-to-have

  • Cross-functional team collaboration skills
  • Continuous quality improvement leadership
  • Electronic system inspection experience
  • Vendor and inventory management skills

Key Requirements

  • Master's degree in Biotechnology or related field
  • 2 years of experience in DI/QC & Admin Lead role
  • Experience with FDA compliant laboratory standards

Work Rights

Not specified

Tailored Resume

Cover Letter